US1398098A - Process for the manufacture of explosives - Google Patents

Process for the manufacture of explosives Download PDF

Info

Publication number
US1398098A
US1398098A US481077A US48107721A US1398098A US 1398098 A US1398098 A US 1398098A US 481077 A US481077 A US 481077A US 48107721 A US48107721 A US 48107721A US 1398098 A US1398098 A US 1398098A
Authority
US
United States
Prior art keywords
explosive
boiling
lead
oxid
manufacture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US481077A
Inventor
Hawkins Thomas
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHAUNCEY R H REX
Original Assignee
CHAUNCEY R H REX
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CHAUNCEY R H REX filed Critical CHAUNCEY R H REX
Priority to US481077A priority Critical patent/US1398098A/en
Application granted granted Critical
Publication of US1398098A publication Critical patent/US1398098A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/04Compositions containing a nitrated organic compound the nitrated compound being an aromatic

Definitions

  • the present invention relates to an improved high-explosive compound, which is also suitable for use as a detonator compositionor as an ingredient thereof, and the process of making such material.
  • a starting material from which the explosive is prepared I preferably use picric acid (trinitrophenol). This is dissolved in water, preferably boiling water, and while boiling, an oxid of lead, such as ordinary scale litharge or red lead, can be used. The mass is kept boiling for a short period, and is then allowed to settle and the filtrate and the precipitate and excess of lead oxid are separated in any other manner.
  • picric acid trinitrophenol
  • a solution of a nitrate, preferably potassium nitrate (or some other non-deliquescent or non-hygroscopic nitrate preferably employed) is then added, which causes a precipitation of the explosive compound.
  • the resulting mass which may be in a paste form, is then placed on a fine filter, and as much water as possible removed by filtration. The material is then dried, at a temperature not above the boiling point of water.
  • This solid material constitutes the base of the explosive compound. It can be compressed into pellets, or into metal cylinders of any suitable size. to be used as a detonator compound for blasting. It can also be used as a high explosive in a similar manner.
  • the detonator is fired in the same manner as fulminate of mercury, as a substitute therefor.
  • nitro-glycerin may be incorporated therewith.
  • Any desired damp-proofing composition may be employed to protect the composition from moisture.
  • the composition can be desensitized by incorporating desensitizing agents, such as nitro-kerosene, mixed with a small amount of nitro-glycerin if desired, or the composition containing the solid material and nitro-glycerin can be desensitized by the employment of nitro-kerosene.
  • the compound is much easier and much safer to manufacture and handle than is fulminate of mercury. It can be substituted for fulminate of mercury in all of the compositions in which the latter is used.
  • other explosive compounds can be incorporated therewith particularly when the same is to be used as a propellant powder or as a blasting powder. It has no effect on metals, and is safe in mines even when the mines contain considerable gas.
  • One of the objects of the introduction of the oxid of lead is to neutralize and combine with the mineral acids and the impurities which may be contained in the picric acid. If these materials were allowed to remain in the picric acid they would be detrimental, for example they would under some conditions absorb moisture and thereby destroy the detonating and explosive properties.
  • the dry product above referred to can be treated to further increase the explosive properties.
  • fuming nitric acid of a gravity for example, fuming nitric acid of a gravity
  • may be used of 1.5 to one molecular part of the finished dry high explosive is added four molecular parts of fuming nitric acid of gravity of 1.5, and the whole allowed to stand for an hour, with occasional stirring at intervals.
  • the free acid is drawn off, the deposit remaining may be again dissolved in boiling water, and treated in a manner similar to thatabove described.
  • I claim ,l The herein described detonating and explosive. compound comprising the reaction product of picric acid, a lead oXid, and a soluble nitrate. 2. The herein described detonating and explosive compound comprising the reaction product of picric acid, a lead oxid, and a soluble nitrate, together with other nitro compounds.
  • the herein described detonating and explosive compound comprising the reaction'product of picric acid, a lead oxid, and a soluble nitrate, renitrated.
  • a process which comprisesdissolving picric acid, adding a ;lead oxid thereto, allowing reaction to take place, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein.
  • a process which comprises dissolving piicric acid, adding a lead oX-id thereto, maintaining the liquid at a boiling temperature until the reaction is completed, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein.
  • a process which comprises dissolving picric acid, adding a lead oxid thereto, maintaining the liquid at a boiling temperature until the reaction is completed, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein,.and thereafter further nitrating the latter.

Description

. umrao srarrs PATEN T OFFICE.
THO MAS HAWKINS, 0F SLATINGTON, PENNSYLVANIA, ASSIGNOR OF ONE-HALF TO CHAUNCEY R. H. REX, OF SLA'IING'ION, PENNSYLVANIA.
reconss FOR THE MANUFACTURE OF 'EXPLOSIVES,
No Drawing.
1 0 (112 whom it may concern:
Be it known that I, THOMAS HAWKINS, a subject of the King of England, residing at Slatington, in the county of Lehigh and State of Pennsylvania, have invented new and useful Improvements in Processes for the Manufacture of Explosives, of which the following is a specification.
The present invention relates to an improved high-explosive compound, which is also suitable for use as a detonator compositionor as an ingredient thereof, and the process of making such material.
As a starting material from which the explosive is prepared, I preferably use picric acid (trinitrophenol). This is dissolved in water, preferably boiling water, and while boiling, an oxid of lead, such as ordinary scale litharge or red lead, can be used. The mass is kept boiling for a short period, and is then allowed to settle and the filtrate and the precipitate and excess of lead oxid are separated in any other manner.
A solution of a nitrate, preferably potassium nitrate (or some other non-deliquescent or non-hygroscopic nitrate preferably employed) is then added, which causes a precipitation of the explosive compound. The resulting mass, which may be in a paste form, is then placed on a fine filter, and as much water as possible removed by filtration. The material is then dried, at a temperature not above the boiling point of water.
As a specific example of the invention, to which the claims are not limited, the following is given:
1 lb. of picric acid (trinitrophenol) is dissolved in 2 gallons of water, preferably boiling, or is heated to boiling. While the boiling operation is continued, there is added, in small quantities, at intervals, 3 lbs. of scale litharge, oxid of lead, or ordinary red lead oxid, in the form of a powder.
The liquid is kept boiling during this opera- Specification of Letters Patent. I Pate ted N 22 1921 Application filed June 28, 1921.
Serial No. 481,077.
chemical reaction which precipitates the whole composition in the form of a paste. This paste or resulting reaction product is then placed on a fine filter, suction'applied if desired, to remove as much of the adherent liquor as possible. The solid material resulting isthen dried, at a temperature not above 100 C.
' This solid material constitutes the base of the explosive compound. It can be compressed into pellets, or into metal cylinders of any suitable size. to be used as a detonator compound for blasting. It can also be used as a high explosive in a similar manner.
The detonator is fired in the same manner as fulminate of mercury, as a substitute therefor.
In order to increase the sensitiveness of the product, a small amount, say 2% or so, of nitro-glycerin may be incorporated therewith. Any desired damp-proofing composition may be employed to protect the composition from moisture. The composition can be desensitized by incorporating desensitizing agents, such as nitro-kerosene, mixed with a small amount of nitro-glycerin if desired, or the composition containing the solid material and nitro-glycerin can be desensitized by the employment of nitro-kerosene. The compound is much easier and much safer to manufacture and handle than is fulminate of mercury. It can be substituted for fulminate of mercury in all of the compositions in which the latter is used. It is to be understood that other explosive compounds can be incorporated therewith particularly when the same is to be used as a propellant powder or as a blasting powder. It has no effect on metals, and is safe in mines even when the mines contain considerable gas.
One of the objects of the introduction of the oxid of lead is to neutralize and combine with the mineral acids and the impurities which may be contained in the picric acid. If these materials were allowed to remain in the picric acid they would be detrimental, for example they would under some conditions absorb moisture and thereby destroy the detonating and explosive properties.
The dry product above referred to can be treated to further increase the explosive properties. by being re-nitrated, for example with fuming nitric acid of a gravity and may be used of 1.5. In this operation, to one molecular part of the finished dry high explosive is added four molecular parts of fuming nitric acid of gravity of 1.5, and the whole allowed to stand for an hour, with occasional stirring at intervals. The free acid is drawn off, the deposit remaining may be again dissolved in boiling water, and treated in a manner similar to thatabove described.
I claim ,l. The herein described detonating and explosive. compound comprising the reaction product of picric acid, a lead oXid, and a soluble nitrate. 2. The herein described detonating and explosive compound comprising the reaction product of picric acid, a lead oxid, and a soluble nitrate, together with other nitro compounds.
3. The herein described detonating and explosive compound comprising the reaction'product of picric acid, a lead oxid, and a soluble nitrate, renitrated.
4. A process which comprisesdissolving picric acid, adding a ;lead oxid thereto, allowing reaction to take place, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein.
5. A process which comprises dissolving piicric acid, adding a lead oX-id thereto, maintaining the liquid at a boiling temperature until the reaction is completed, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein.
6. A process which comprises dissolving picric acid, adding a lead oxid thereto, maintaining the liquid at a boiling temperature until the reaction is completed, removing undissolved material, adding a soluble nitrate, separating aqueous liquid from the solid material present therein,.and thereafter further nitrating the latter.
In testimony whereof I have ailixed my signature.
THOMAS HAWKINS.
US481077A 1921-06-28 1921-06-28 Process for the manufacture of explosives Expired - Lifetime US1398098A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US481077A US1398098A (en) 1921-06-28 1921-06-28 Process for the manufacture of explosives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US481077A US1398098A (en) 1921-06-28 1921-06-28 Process for the manufacture of explosives

Publications (1)

Publication Number Publication Date
US1398098A true US1398098A (en) 1921-11-22

Family

ID=23910489

Family Applications (1)

Application Number Title Priority Date Filing Date
US481077A Expired - Lifetime US1398098A (en) 1921-06-28 1921-06-28 Process for the manufacture of explosives

Country Status (1)

Country Link
US (1) US1398098A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2973257A (en) * 1951-06-14 1961-02-28 Olin Mathieson Propellent powder

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2973257A (en) * 1951-06-14 1961-02-28 Olin Mathieson Propellent powder

Similar Documents

Publication Publication Date Title
CA2227625C (en) Method of preparing dinitramidic acid and salts thereof
US3138496A (en) Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax
EP3066054B1 (en) Bismuth-based energetic materials
US2406572A (en) Explosive perchlorates of aliphatic nitrogenous compounds
US1398098A (en) Process for the manufacture of explosives
US3278350A (en) Explosive-ammonium nitrate in phenol-aldehyde resin
US2371879A (en) Explosive charge
US3269879A (en) Ammonium salt lattice with isomorphously substituted inorganic salts
US3147160A (en) Desensitization of ammonium perchlorate
US4112220A (en) Nitrate esters of galactomannan gums and methods for their synthesis
US2929698A (en) Explosive
US1580572A (en) Manufacture of detonating compositions
US4047989A (en) Method for the recovery of blasting oil from effluents from the production of nitroglycerine-containing explosives
US1552836A (en) Priming composition and process for producing the same
US2195551A (en) Explosive
US1371215A (en) Explosive and process of making explosives
US2989389A (en) Primer charge for detonators
US3002012A (en) Method for the preparation of normal lead styphnate
US3714260A (en) 4,4-bis (difluoramino)-1,7-difluoro-1,1,7,7-tetranitroheptane
US1914530A (en) Method of producing noncrystalline explosive azide
US2415001A (en) Explosive compounds
US1206223A (en) Process of making glycol dinitrate for explosive uses.
US1922123A (en) Inulin nitrate and method of producing
US1424462A (en) Process for the manufacture of detonating caps for mining and military purposes
US1503956A (en) Explosive and process of making same